methyl 5-cyano-1-methyl-1H-pyrazole-3-carboxylate

methyl 5-cyano-1-methyl-1H-pyrazole-3-carboxylate

methyl 3-(tert-butoxymethyl)-1H-pyrazole-4-carboxylate

methyl 3-(tert-butoxymethyl)-1H-pyrazole-4-carboxylate

methyl 5-(hydroxymethyl)-1H-pyrazole-4-carboxylate

$300.00
CAS No.: 2383801-05-4
Catalog No.: 192874
Purity: 95%
MF: C6H8N2O3
MW: 156.141
Storage: 2-8 degree Celsius
SMILES: OCC1=C(C=NN1)C(=O)OC
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methyl 5-(hydroxymethyl)-1H-pyrazole-4-carboxylate; CAS No.: 2383801-05-4; methyl 5-(hydroxymethyl)-1H-pyrazole-4-carboxylate. PROPERTIES: This compound appears as a white crystalline solid with molecular formula C7H8N2O3 and a molecular weight of 164.15 g/mol. It demonstrates a melting point in the range of 142-146 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to oxidation and should be stored under inert atmosphere. Recommended storage involves maintaining in tightly sealed containers at temperatures below 20 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as methyl 5-(hydroxymethyl)-1H-pyrazole-4-carboxylate may cause skin irritation. The hydroxymethyl group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, methyl 5-(hydroxymethyl)-1H-pyrazole-4-carboxylate serves as an intermediate for synthesizing antiviral agents, as described in medicinal chemistry literature focusing on nucleoside analogs. Its hydroxymethyl substituent enables formation of glycosidic bonds in carbohydrate chemistry. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through esterification reactions. Academic research has explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The pyrazole ring system also facilitates coordination with metal ions, making it valuable for creating coordination polymers in materials science applications, as evidenced by structural chemistry publications.

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